Stéphane Rousseau

APP, PSEN1, and PSEN2 mutations in early-onset Alzheimer disease: A genetic screening study of familial and sporadic cases

Hélène-Marie Lanoiselée, Gaël Nicolas, David Wallon et al. · PLoS Medicine · 2017 · 609 citations · Full text

Life Sciences, Genetics, Neurology +17

Mutation of the <i>PDGFRB</i> gene as a cause of idiopathic basal ganglia calcification

Gaël Nicolas, Cyril Pottier, David Maltête et al. · Neurology · 2012 · 277 citations

Life Sciences, Genetics, Molecular Genetics +17

Phenotypic spectrum of probable and genetically-confirmed idiopathic basal ganglia calcification

Gaël Nicolas, Cyril Pottier, Camille Charbonnier et al. · Brain · 2013 · 233 citations · Full text

Medicine, Neurology, Neuroscience +12

Contribution to Alzheimer's disease risk of rare variants in TREM2, SORL1, and ABCA7 in 1779 cases and 1273 controls

Céline Bellenguez, Camille Charbonnier, Benjamin Grenier‐Boley et al. · Neurobiology of Aging · 2017 · 170 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

TREM2 R47H Variant as a Risk Factor for Early-Onset Alzheimer's Disease

Cyril Pottier, David Wallon, Stéphane Rousseau et al. · Journal of Alzheimer s Disease · 2013 · 164 citations

Life Sciences, Genetics, Molecular Genetics +15